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À propos
All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description.
This role sits within a growing MES team supporting Electronic Batch Records, Weigh & Dispense, and equipment logbooks in a highly regulated biotech manufacturing environment.
Key Responsibilities
Design and configure Electronic Batch Records (EBR)
Support MES Weigh & Dispense and Equipment Management modules
Collaborate closely with shop floor operations
Deliver MES projects from discovery through to go-live in line with GMP
Maintain integrations across ERP, automation, and lab systems
Troubleshoot and enhance system performance
Participate in an on-call support rota
Experience Required
5+ years in a GMP-regulated environment
Strong MES experience, ideally Emerson Syncade
Proven background in validation, testing, and COTS implementations
Knowledge of biotech/pharma manufacturing processes
Exposure to PLC, DCS, or SCADA systems
Experience with Visual Basic and MS SQL Server (advantageous)
Understanding xcfaprz of ITIL and MES-ERP integrations
Profile
Strong communicator with client‑facing experience
Comfortable working cross‑functionally in agile environments
Proactive, detail‑oriented, and delivery‑focused
If you’re interested in working on high‑impact digital manufacturing systems within a global pharma environment, feel free to reach out directly.
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Compétences linguistiques
- English
Avis aux utilisateurs
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